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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148032insertion1nstd232human GRCh37.p13 chr1: 220,179,654-220,179,654 , GRCh38.p12 chr1: 220,006,312-220,006,312 EPRS1
    nsv7147807insertion1nstd232human GRCh37.p13 chr1: 220,193,563-220,193,563 , GRCh38.p12 chr1: 220,020,221-220,020,221 EPRS1
    nsv7147148insertion1nstd232human GRCh37.p13 chr1: 220,142,466-220,142,466 , GRCh38.p12 chr1: 219,969,124-219,969,124 EPRS1
    nsv7146414copy number variation1nstd232human GRCh37.p13 chr1: 220,142,297-220,142,397 , GRCh38.p12 chr1: 219,968,955-219,969,055 EPRS1
    nsv7145121insertion1nstd232human GRCh37.p13 chr1: 220,153,584-220,153,584 , GRCh38.p12 chr1: 219,980,242-219,980,242 EPRS1
    nsv7144919insertion1nstd232human GRCh37.p13 chr1: 220,179,655-220,179,655 , GRCh38.p12 chr1: 220,006,313-220,006,313 EPRS1
    nsv7144352insertion1nstd232human GRCh37.p13 chr1: 220,192,422-220,192,422 , GRCh38.p12 chr1: 220,019,080-220,019,080 EPRS1
    nsv7141359insertion1nstd232human GRCh37.p13 chr1: 220,146,740-220,146,740 , GRCh38.p12 chr1: 219,973,398-219,973,398 EPRS1
    nsv7140177insertion1nstd232human GRCh37.p13 chr1: 220,156,742-220,156,742 , GRCh38.p12 chr1: 219,983,400-219,983,400 EPRS1
    nsv7139670insertion1nstd232human GRCh37.p13 chr1: 220,170,687-220,170,687 , GRCh38.p12 chr1: 219,997,345-219,997,345 EPRS1
    nsv7138426insertion1nstd232human GRCh37.p13 chr1: 220,178,703-220,178,703 , GRCh38.p12 chr1: 220,005,361-220,005,361 EPRS1
    nsv7137885insertion1nstd232human GRCh37.p13 chr1: 220,154,200-220,154,200 , GRCh38.p12 chr1: 219,980,858-219,980,858 EPRS1
    nsv7099262copy number variation1nstd231human GRCh38.p12 chr1: 211,826,028-221,140,287 , GRCh37 chr1: 211,999,370-221,313,629 ATF3, CENPF, 114 more genes
    nsv7095973copy number variation1nstd102humanPathogenic GRCh37 chr1: 220,088,791-220,445,679 , GRCh38.p12 chr1: 219,915,449-220,272,337 AURKAP1, IARS2, 13 more genes
    nsv7095972copy number variation1nstd102humanPathogenic GRCh37 chr1: 218,520,044-220,986,760 , GRCh38.p12 chr1: 218,346,702-220,813,418 TGFB2, LOC105373475, 38 more genes
    nsv7095587copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,088,791-220,986,760 , GRCh38.p12 chr1: 219,915,449-220,813,418 BPNT1, SNORA36B, 24 more genes
    nsv7095512copy number variation1nstd102humanUncertain significance GRCh37 chr1: 220,088,791-220,406,225 , GRCh38.p12 chr1: 219,915,449-220,232,883 MIR215, SNX2P1, 11 more genes
    nsv7052462inversion1nstd229human GRCh38 chr1: 219,653,745-221,511,784 , GRCh37.p13 chr1: 219,827,087-221,685,126 RNA5SP76, MIR215, 36 more genes
    nsv6668840copy number variation1nstd229human GRCh38 chr1: 220,032,456-220,032,631 , GRCh37.p13 chr1: 220,205,798-220,205,973 EPRS1
    nsv6658142copy number variation1nstd229human GRCh38 chr1: 220,012,601-220,117,900 , GRCh37.p13 chr1: 220,185,943-220,291,242 IARS2, LOC105373475, 4 more genes
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